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Structure of 253453-91-7
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2-Chloro-1-methyl-1H-imidazole is a bench-stable, moisture-tolerant heterocyclic reagent featuring a reactive chlorine atom at the 2-position. This electrophilic site enables efficient coupling in nucleophilic substitution reactions, particularly in the synthesis of imidazolium salts and functionalized pharmaceutical intermediates. The methyl group enhances solubility in polar organic solvents while stabilizing the imidazole core under standard handling conditions.
2-Chloro-1-methyl-1H-imidazole serves as a versatile electrophilic imidazole reagent, enabling efficient N-alkylation and heterocycle functionalization under mild conditions. Its bench-stable nature and compatibility with diverse nucleophiles facilitate rapid access to substituted imidazoles, making it a practical building block for medicinal chemistry and catalytic synthesis workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: